Development of a nanoprecipitation method intended for the entrapment of hydrophilic drugs into nanoparticles
- PMID: 15626579
- DOI: 10.1016/j.ejps.2004.09.011
Development of a nanoprecipitation method intended for the entrapment of hydrophilic drugs into nanoparticles
Abstract
This study investigates formulation and process modifications to improve the versatility of the nanoprecipitation technique, particularly with respect to the encapsulation of hydrophilic drugs (e.g. proteins). More specifically, the principal objective was to explore the influence of such modifications on nanoparticle size. Selected parameters of the nanoprecipitation method, such as the solvent and the non-solvent nature, the solvent/non-solvent volume ratio and the polymer concentration, were varied so as to obtain polymeric nano-carriers. The feasibility of such a modified method was assessed and resulting unloaded nanoparticles were characterized with respect to their size and shape. It was shown that the mean particle size was closely dependent on the type of non-solvent selected. When alcohols were used, the final mean size increased in the sequence: methanol<ethanol<propanol. Surfactants added to the dispersing medium were usually unnecessary for final suspension stabilization. Changing the solvent/non-solvent volume ratio was also not a determinant factor for nanoparticle formation and their final characteristics, provided that the final mixture itself did not become a solvent for the polymer. A too high polymer concentration in the solvent, however, prevented nanoparticle formation. Both poly(lactic acid) (PLA) and poly(d,l-lactic-co-glycolic acid) (PLGA) could be used by accurately choosing the polymer solvent and in this respect, some non-toxic solvents with different dielectric constants were selected. The nanoparticles obtained ranged from about 85-560 nm in size. The nanoparticle recovery step however needs further improvements, since bridges between particles which cause flocculation could be observed. Finally, the presented results demonstrate that the nanoprecipitation technique is more versatile and flexible than previously thought and that a wide range of parameters can be modified.
Similar articles
-
Design and optimization of NSAID loaded nanoparticles.Pak J Pharm Sci. 2007 Apr;20(2):157-62. Pak J Pharm Sci. 2007. PMID: 17416573
-
Gelatin nanoparticle preparation by nanoprecipitation.J Biomater Sci Polym Ed. 2011;22(4-6):753-71. doi: 10.1163/092050610X492093. Epub 2010 Jun 21. J Biomater Sci Polym Ed. 2011. PMID: 20566056
-
Nano/micro technologies for delivering macromolecular therapeutics using poly(D,L-lactide-co-glycolide) and its derivatives.J Control Release. 2008 Feb 11;125(3):193-209. doi: 10.1016/j.jconrel.2007.09.013. Epub 2007 Oct 22. J Control Release. 2008. PMID: 18083265 Review.
-
Haloperidol-loaded PLGA nanoparticles: systematic study of particle size and drug content.Int J Pharm. 2007 May 24;336(2):367-75. doi: 10.1016/j.ijpharm.2006.11.061. Epub 2006 Dec 5. Int J Pharm. 2007. PMID: 17207944
-
Nanoprecipitation and the "Ouzo effect": Application to drug delivery devices.Adv Drug Deliv Rev. 2014 May;71:86-97. doi: 10.1016/j.addr.2013.12.009. Epub 2013 Dec 30. Adv Drug Deliv Rev. 2014. PMID: 24384372 Review.
Cited by
-
Association of Thermoresponsive Diblock Copolymer PDEGMA-b-PDIPAEMA in Aqueous Solutions: The Influence of Terminal Groups.Polymers (Basel). 2024 Jul 24;16(15):2102. doi: 10.3390/polym16152102. Polymers (Basel). 2024. PMID: 39125129 Free PMC article.
-
Solvent Controls Nanoparticle Size during Nanoprecipitation by Limiting Block Copolymer Assembly.Macromolecules. 2022 Sep 27;55(18):8040-8048. doi: 10.1021/acs.macromol.2c00907. Epub 2022 Sep 9. Macromolecules. 2022. PMID: 36186573 Free PMC article.
-
Synthesis of prostaglandin E(1) phosphate derivatives and their encapsulation in biodegradable nanoparticles.Pharm Res. 2009 Jul;26(7):1792-800. doi: 10.1007/s11095-009-9891-5. Epub 2009 May 5. Pharm Res. 2009. PMID: 19415470
-
Facile synthesis of biocompatible gold nanoparticles from Vites vinefera and its cellular internalization against HBL-100 cells.Cancer Nanotechnol. 2011;2(1-6):121-132. doi: 10.1007/s12645-011-0022-8. Epub 2011 Sep 15. Cancer Nanotechnol. 2011. PMID: 26316896 Free PMC article.
-
Engineered Nanoplatelets for Enhanced Treatment of Multiple Myeloma and Thrombus.Adv Mater. 2016 Nov;28(43):9573-9580. doi: 10.1002/adma.201603463. Epub 2016 Sep 14. Adv Mater. 2016. PMID: 27626769 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical